Hogewind, B. F., Pennings, R. J., Hol, F. A., Kunst, H. P., Hoefsloot, E. H., Cruysberg, J. R., & Cremers, C. W. (2010). Autosomal dominant optic neuropathy and sensorineual hearing loss associated with a novel mutation of WFS1. Molecular Vision.

Hogewind, Barend F.T., Ronald J.E Pennings, Frans A. Hol, Henricus P.M Kunst, Elisabeth H. Hoefsloot, Johannes R.M Cruysberg, and Cor W.R.J Cremers. Autosomal Dominant Optic Neuropathy and Sensorineual Hearing Loss Associated With a Novel Mutation of WFS1. Molecular Vision, 2010.

Hogewind, Barend F.T., et al. Autosomal Dominant Optic Neuropathy and Sensorineual Hearing Loss Associated With a Novel Mutation of WFS1. Molecular Vision, 2010.